Canonical Allele Identifier: PA916043919
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386884
ClinVar RCV Id: RCV000433329 RCV000765979 RCV001849371 RCV001848781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Arg374Gln
CA4374971
NM_001363671.2:c.1121G>A